硼替佐米用于血管免疫母细胞t细胞淋巴瘤危重患者。

IF 0.7 Q4 HEMATOLOGY Case Reports in Hematology Pub Date : 2022-08-31 eCollection Date: 2022-01-01 DOI:10.1155/2022/6079633
Motoharu Shibusawa
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引用次数: 2

摘要

血管免疫母细胞t细胞淋巴瘤(AITL)占所有外周血t细胞淋巴瘤的18.5%。目前还没有金标准的化疗来治疗新诊断的AITL。本病例描述了在新诊断的AITL中使用硼替佐米。53岁男性,既往无疾病,左颈部出现红斑和肿胀。根据淋巴结活检结果诊断为AITL。AITL进展导致患者一般情况严重恶化。因此给予硼替佐米,导致淋巴结病变减少,肿瘤热消失,血清乳酸脱氢酶水平降低。随后,患者的一般情况逐渐好转。尽管患者病情不佳,但硼替佐米耐受性良好。服用硼替佐米后,患者大约10个月不需要化疗。本病例表明硼替佐米是AITL患者的一种可能的治疗选择。
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Bortezomib Use for a Critically Ill Patient with Angioimmunoblastic T-Cell Lymphoma.

Angioimmunoblastic T-cell lymphoma (AITL) accounts for 18.5% of all peripheral T-cell lymphomas. There is still no gold standard chemotherapy for treating newly diagnosed AITL. This case describes the use of bortezomib in newly diagnosed AITL. A 53-year-old man with no previous illness presented with erythema and swelling in the left neck. A diagnosis of AITL was made based on the results of lymph node biopsies. AITL progression led the patient to a severely deteriorated general condition. Bortezomib was thus administered, which resulted in a reduction in lymphadenopathies, the disappearance of tumor fever, and a decrease in serum lactate dehydrogenase levels. Subsequently, the patient's general condition gradually improved. Despite the patient's poor condition, bortezomib was well tolerated. After bortezomib administration, the patient did not require chemotherapy for approximately 10 months. The present case indicates that bortezomib is a possible treatment option for patients with AITL.

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